A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015216



Internal ID19104433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61605421..61961244hg38UCSC Ensembl
Innerchr8:62517980..62873803hg19UCSC Ensembl
Innerchr8:62680534..63036357hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38355824
hg19355824
hg18355824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689471
Samples
Known GenesASPH, MIR4470
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015216
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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